Data / Medical devices / Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) / Mexico
FDA-registered makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) in Mexico: 6 establishments
6 establishments in Mexico are registered with the FDA to make Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) (product code MWI). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- Product code
- MWI
- Country
- Mexico
Makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Industrial Vallera de Mexicali, S. A. de C. V. | Mexicali Mexico, Mexico | Manufacturer | 7 | August 12, 2026 | 0 | 0 | 0 | api.fda.gov |
| GE Medical Systems Information Technologies - Critikon de Mexico S. de R.L. de C.V. | JUAREZ Chihuahua, Mexico | Manufacturer | 4 | April 25, 2024 | 0 | 0 | 0 | api.fda.gov |
| Industrial Vallera de Mexicali, S.A. de C.V. (Terra) | Mexicali Baja California, Mexico | Manufacturer | 4 | August 12, 2026 | 0 | 0 | 0 | api.fda.gov |
| Amphenol Alden Products Company | Hermosillo Sonora, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hi-Tech Products De Mexico S.A. De C.V. | La Mesa, Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Velcromex, S.A. De C.V. | AGUA PRIETA Sonora, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.